Dual Strain-Promoted Alkyne–Nitrone Cycloadditions for Simultaneous Labeling of Bacterial Peptidoglycans
Author:
Affiliation:
1. Life Sciences Division, National Research Council of Canada, 100 Sussex Drive, Ottawa K1A 0R6, Canada
2. Department of Chemistry and Biomolecular Sciences, University of Ottawa, 10 Marie Curie, Ottawa K1N 6N5, Canada
Funder
Government of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.6b00063
Reference33 articles.
1. Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality
2. Chemical reporters for biological discovery
3. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
4. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides
5. Cellular Lipid Metabolism Is Influenced by the Coordination Environment of Copper
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